LUISA now has remote monitoring! Through the prisma CLOUD platform with a cellular modem, the LUISA ventilator allows for on-demand remote monitoring access to help manage your patients’ treatment simply and securely. The prisma CLOUD platform is a HIPAA-compliant, U.S.-based Microsoft Azure data center.
Attached are the instructions to install the firmware update. Please note there is also a battery update included in the firmware file. The firmware file will be available for download on the Movair customer portal by end of day, or, contact us and we can send a USB-c with the firmware update. Please see attached for list of updates included with this firmware file.
It has never been easier to follow your patients whenever you need to with LUISA’s cellular modem.
• The modem easily attaches the LUISA device handle for convenience and easy travel when needed
• The modem is plugged in and powered by the LUISA so there is no need to find another outlet near the bedside or anywhere else for monitoring
• The modem goes where LUISA goes so wherever the patient is the modem and remote monitoring are there and available
The prisma CLOUD platform automatically ensures access to all relevant therapy data at all times. Your care teams can track usage, view trends and key therapy results simply and securely. Simple-to-use and fully automatic remote monitoring from anywhere grants you an opportunity for increased efficiency in your patients care.
With over 20,000 units sold LUISA is a proven and preferred home ventilator. LUISA utilizes all standard volume, pressure, and mouthpiece ventilation modes with the added benefit of High Flow Therapy. LUISA’s targeted tidal volume mode (TTV-VAPS-AE) also offers unique and proprietary comfort settings designed to help improve therapy and patient compliance.
• Sensitive Inspiratory and Expiratory Triggers with Inspiratory Lock Out Time
• Three Target Volume Speeds
• Pressure Increase/Rise and Pressure Reduction/Drop
• Flow-Based Auto-EPAP
• Auto-Rate algorithm
The LUISA has been authorized by the FDA under an EUA but has not been FDA cleared or approved. The LUISA is authorized only for the duration of the declaration that circumstances exist justifying the authorization of the emergency use under section 564(b)(1) of the Act, 21 U.S.C. § 360bbb-3(b)(1), unless the authorization is terminated or revoked sooner. U.S. federal law restricts this device to sale by or on the order of a physician.
